This work was supported by JSPS KAKENHI grant number JP18K14260 and the budget of Japan Agency for Marine-Earth Science and Technology. We thank Shigeru Deguchi (JAMSTEC) and Tetsuro Ikuta (JAMSTEC) for providing the characterization facilities. We thank Ken Takai (JAMSTEC) for commercial software support. The microfabrication was conducted at Takeda Sentanchi Supercleanroom, The University of Tokyo, supported by &#34;Nanotechnology Platform Program&#34; of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, Grant Number JPMXP09F19UT0087.

1. Microfabrication of the femtoliter microchamber array substrate
NOTE: Conduct the following microfabrication experiment in a cleanroom. Wear gloves and a cleanroom suit before entering the cleanroom.
<ol>
	<li>Cleaning cover glass substrate
	<ol>
		<li>Set the cover glass on a cover glass staining rack. Sonicate the cover glass in 8 M sodium hydroxide (NaOH) for 15 min at room temperature (RT). 
		CAUTION: NaOH in high concentrations is highly dangerous to skin and eye. Gently handle...

The authors have nothing to disclose.

The highly quantitative measurement based on the highly uniform, stable, and biocompatible droplets in FemDA enabled the discrete distribution, the unique feature of our study differing from others. We systematically optimized and detailed the microfabrication and droplet formation processes in this paper. There are several critical steps in the established protocol.
First, the uniform coating of highly viscous CYTOP polymer on the rectangular thin glass substrate largely determines the qualit...

Researchers use reactors to carry out bio/chemical reactions. There are significant efforts that have been made to reduce the size of the reactor and increase the experimental throughput in order to lower the reagent consumption while improving the work efficiency. Both aspects aim to liberate researchers from a heavy workload, decreasing the cost and speeding up research and development. We have a clear historical roadmap about the development of the reactor technologies from the viewpoint of reaction volumes and throughput: single beakers/flask/test-tubes, milliliter tubes, microliter tubes, microliter 8-tube strips, microliter 96/384/1536-well plate, and microfluidic nanoliter/picoliter/femtoliter reactors1,2,3,4,5,6,7. Analogous to downsizing the feature size of transistors on integrated circuit chips in the semiconductor industry in the past decades, bio/chemical microreactors are going through volume reduction and system integration. Such small-scale tools have had a profound impact on cell-based or cell-free synthetic biology, biomanufacturing, and high-throughput prototyping and screening8,9,10,11,12. This paper describes our recent effort on the development of a unique droplet array technology and demonstrates its application in CFPS13, a fundamental technology for synthetic biology and molecular screening communities14. In particular, we intentionally provide an optimized and low-cost protocol to make the FemDA device accessible to everyone. The low-cost and easy-to-handle protocol for the miniaturized device would contribute to the educational purposes of universities and help spread the technology.
FemDA prepares femtoliter droplets at an ultrahigh density of 106 per 1 cm2 on a planar glass substrate. We coated a hydrophobic polymer, CYTOP15, on the glass substrate and selectively etched (removed) CYTOP at predefined positions to generate a microchamber array on the substrate. Thus, the resulting microchamber is composed of a hydrophobic sidewall (CYTOP) and a hydrophilic bottom (glass). When sequentially flowing water and oil over the patterned surface, the water can be trapped and sealed into the microchambers. The hydrophilic-in-hydrophobic structure is vital for repelling water outside the microchambers, isolating individual microreactors, and retaining a tiny aqueous solution inside the femtoliter space. The unique property was successfully applied for the preparation of water-in-oil droplets and lipid bilayer microcompartments16,17. Compared to the prototype device16, we first optimized the microfabrication process to realize a complete removal of the CYTOP polymer as well as a full exposure of the glass bottom. CYTOP is a special fluoropolymer featuring extremely low surface tension (19 mN/m) lower than that of conventional microreactor materials such as glass, plastics, and silicone. Its good optical, electrical, and chemical performance have already been utilized in surface treatment of microfluidic devices18,19,20,21,22,23,24. In the FemDA system, to achieve good wetting of the oil on the CYTOP surface, the surface tension of the oil must be lower than that of the solid surface25. Otherwise, the liquid oil in contact with the solid surface tends to become spherical rather than spreading over the surface. Besides, we found that some popular perfluorocarbon oils (e.g., 3M FC-40)16 and hydrofluoroether oils (e.g., 3M Novec series) can dissolve CYTOP as a result of the amorphous morphology of CYTOP, which is fatal to quantitative measurement and would be questionable in terms of cross-contamination among droplets. Fortunately, we identified a biocompatible and environmentally friendly oil exhibiting lower (&#60; 19 mN/m) surface tension13. We also found a new surfactant that can dissolve in the selected oil and function in a low concentration (0.1%, at least 10-fold lower than previously reported popular ones26,27)13. The resulting water/oil interface can be stabilized by the surfactant. Because of the high evaporation rate of the oil, following the flush with the oil, we applied another biocompatible and environmentally friendly oil to replace the first one to seal the microchambers. We call the first oil (ASAHIKLIN&#160;AE-3000 with 0.1 wt % SURFLON S-386) the &#8220;flush oil&#8221; and the second oil (Fomblin Y25) the &#8220;sealing oil,&#8221; respectively.
The two-step oil-sealing strategy can realize a robust formation of the femtoliter droplet array within minutes and without sophisticated instrumentation. Due to the evaporation problem, it has been considered challenging to generate microreactors smaller than picoliter volumes28. FemDA addressed this issue by systematically optimizing the materials and processes used for the preparation of microreactors/droplets. Several noteworthy features of the resulting droplets include the high uniformity (or monodispersity), stability, and biocompatibility at the femtoliter scale. The coefficient of variation (CV) of the droplet volume is only 3% (without vignetting correction for the microscopic images), the smallest CV among droplet platforms in the world, which ensures a highly parallel and quantitative measurement. The femtoliter droplet is stable for at least 24 hours without cross-contamination among droplets at room temperature, which is valuable for a reliable time-course measurement. Regarding the biocompatibility, we succeeded in synthesizing various proteins from a single-copy template DNA in the femtoliter droplet, which had previously been considered difficult or inefficient29,30. It would be worthy of elucidating why some proteins capable of being synthesized in the FemDA cannot be synthesized in other droplet systems. FemDA was not merely a technical advancement, but also realized an unprecedentedly quantitative measurement that can correlate the protein yield (as reflected by the fluorescence intensity of the droplet) to the number of template DNA molecules in each droplet. As a result, the histogram of the fluorescence intensity of droplets from FemDA-based CFPS showed a discrete distribution that can be nicely fitted by a sum of Gaussian distributions of equal peak-to-peak intervals. Moreover, the probability of occurrence of droplets containing different numbers of DNA molecules was a perfect fit to a Poisson distribution31. Thus, the different protein yield in each droplet can be normalized based on the discrete distribution. This critical feature allows us to separate the enzymatic activity information from the apparent intensity, that has not been available with other microreactor platforms yet. Existing microfluidic cell/droplet sorting systems are skilled in fully automatic sorting and good at concentrating samples but sometimes can only output a relatively broad or long-tailed histogram in the analytical aspect32,33. Our highly quantitative and biocompatible FemDA system sets a new benchmark and a high analytical standard in the field of microreactor development.
The oils and surfactants that could be used for the preparation of droplets are still very limited34. The combination of ASAHIKLIN AE-3000 and SURFLON S-386 established in FemDA is a new member of the growing arsenal of the physiochemical interface between the aqueous phase and the oil phase13. The new interface in FemDA is physically stable, chemically inert, and biologically compatible with the complex transcription, translation, and post-translational modification machinery for many sorts of proteins13. It would be rather attractive to find a protein that cannot be synthesized in the droplet settings instead. Besides, the cost saving of reagents is more evident in the femtoliter droplet system than that in nanoliter and picoliter reactor systems35,36. In particular, there would often be a large dead volume, which is mainly caused by tubing or external supplies, in microfluidic droplet generation systems but not in our FemDA. The array format is also favored by repeated and detailed microscopic characterization (similar to so-called high-content analysis) for every single reactor37, rather than only a single snapshot for a fast-moving object. The femtoliter scale enabled the integration of over one million reactors on a finger-sized area, while the same number of nanoliter reactors (if it exists) requires over square meter area, which would be undoubtedly impractical to manufacture or use such system.

<table>
	<tbody>
		<tr>
			<td>(3-aminopropyl)triethoxysilane</td>
			<td>Sigma-Aldrich</td>
			<td>440140</td>
			<td></td>
		</tr>
		<tr>
			<td>1 mL syringe</td>
			<td>Terumo</td>
			<td>SS-01T</td>
			<td></td>
		</tr>
		<tr>
			<td>2-propanol</td>
			<td>Kanto Chemical</td>
			<td>EL grade</td>
			<td>EL: for electronic use.</td>
		</tr>
		<tr>
			<td>3D laser scanning confocal microscope</td>
			<td>Lasertec</td>
			<td>OPTELICS HYBRID</td>
			<td>Other similar microscopes (e.g., Keyence VK-X1000, Olympus LEXT OLS5000) are also applicable.</td>
		</tr>
		<tr>
			<td>50 mL syringe</td>
			<td>Terumo</td>
			<td>SS-50LZ</td>
			<td></td>
		</tr>
		<tr>
			<td>6,8-difluoro-4-methylumbelliferyl phosphate</td>
			<td>Thermo Fisher Scientific</td>
			<td>D6567</td>
			<td>Prepare a 5 mM stock solution in dimethyl sulfoxide</td>
		</tr>
		<tr>
			<td>Acetone</td>
			<td>Kanto Chemical</td>
			<td>EL grade</td>
			<td>EL: for electronic use. 
			Purity 99.8%.</td>
		</tr>
		<tr>
			<td>Air blower</td>
			<td>Hozan</td>
			<td>Z-263</td>
			<td></td>
		</tr>
		<tr>
			<td>Aluminum block</td>
			<td>BIO-BIK</td>
			<td>AB-24M-02</td>
			<td></td>
		</tr>
		<tr>
			<td>Aluminum microtube stand</td>
			<td>BIO-BIK</td>
			<td>AB-136C</td>
			<td></td>
		</tr>
		<tr>
			<td>ASAHIKLIN AE-3000</td>
			<td>AGC</td>
			<td>(Test sample)</td>
			<td>Free test sample may be available upon inquiry to AGC.</td>
		</tr>
		<tr>
			<td>BEMCOT PS-2 wiper</td>
			<td>Ozu</td>
			<td>028208</td>
			<td></td>
		</tr>
		<tr>
			<td>Biopsy punch with plunger</td>
			<td>Kai</td>
			<td>BPP-10F</td>
			<td></td>
		</tr>
		<tr>
			<td>Cover glass</td>
			<td>Matsunami Glass</td>
			<td>No. 1 (24 mm &#215; 32 mm, 0.13~0.17 mm thickness)</td>
			<td>Size-customized.</td>
		</tr>
		<tr>
			<td>Cover glass staining rack</td>
			<td>Nakayama</td>
			<td>803-131-11</td>
			<td></td>
		</tr>
		<tr>
			<td>CRECIA TechnoWipe clean wiper</td>
			<td>Nippon Paper Crecia</td>
			<td>C100-M</td>
			<td></td>
		</tr>
		<tr>
			<td>Cutting mat</td>
			<td>GE Healthcare</td>
			<td>WB100020</td>
			<td></td>
		</tr>
		<tr>
			<td>CYTOP</td>
			<td>AGC</td>
			<td>CTL-816AP</td>
			<td></td>
		</tr>
		<tr>
			<td>Deaeration mixer</td>
			<td>Thinky</td>
			<td>AR-100</td>
			<td></td>
		</tr>
		<tr>
			<td>Desktop cutter</td>
			<td>Roland</td>
			<td>STIKA SV-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Developer</td>
			<td>AZ Electronic Materials</td>
			<td>AZ 300 MIF</td>
			<td>AZ Electronic Materials was now acquired by Merck. 
			Other alkaline developers may be also applicable but should require optimization of development conditions (time, temperature, etc.)</td>
		</tr>
		<tr>
			<td>Double-coated adhesive Kapton film tape</td>
			<td>Teraoka Seisakusho</td>
			<td>7602 #25</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>Kanto Chemical</td>
			<td>EL grade</td>
			<td>EL: for electronic use. 
			Purity 99.5%.</td>
		</tr>
		<tr>
			<td>Fiji</td>
			<td></td>
			<td></td>
			<td>Version: ImageJ 1.51n</td>
		</tr>
		<tr>
			<td>Flat-cable cutter</td>
			<td>Tokyo-IDEAL</td>
			<td>MT-0100</td>
			<td></td>
		</tr>
		<tr>
			<td>Fomblin oil</td>
			<td>Solvay</td>
			<td>Y25, or Y25/6</td>
			<td>Free test sample may be available upon inquiry to Solvay. Fomblin Y25/6 is an alternative if Y25 is not readily available.</td>
		</tr>
		<tr>
			<td>Hot plate</td>
			<td>AS ONE</td>
			<td>TH-900</td>
			<td></td>
		</tr>
		<tr>
			<td>Injection needle</td>
			<td>Terumo</td>
			<td>NN-2270C</td>
			<td>22G &#215; 70 mm</td>
		</tr>
		<tr>
			<td>Inverted fluorescence microscope</td>
			<td>Nikon</td>
			<td>Eclipse Ti-E</td>
			<td>Epifluorescence specification, CCD or sCMOS camera, motorized stage, autofocus system, and high NA objective lens are required.</td>
		</tr>
		<tr>
			<td>KaleidaGraph</td>
			<td>Synergy</td>
			<td></td>
			<td>Version: 4.5</td>
		</tr>
		<tr>
			<td>Mask aligner</td>
			<td>SUSS</td>
			<td>MA-6</td>
			<td>Other mask aligners are also applicable as long as the vacuum contact mode is avaliable.</td>
		</tr>
		<tr>
			<td>MICROMAN pipette</td>
			<td>GILSON</td>
			<td>E M250E</td>
			<td>Capillary piston tip: CP250</td>
		</tr>
		<tr>
			<td>Microsoft Excel</td>
			<td>Microsoft</td>
			<td></td>
			<td>Version: 16.16.15</td>
		</tr>
		<tr>
			<td>Mini vacuum chamber</td>
			<td>AS ONE</td>
			<td>MVP-100MV</td>
			<td></td>
		</tr>
		<tr>
			<td>Nuclease-free water</td>
			<td>NIPPON GENE</td>
			<td>316-90101</td>
			<td></td>
		</tr>
		<tr>
			<td>Parafilm</td>
			<td>Amcor</td>
			<td>PM-996</td>
			<td></td>
		</tr>
		<tr>
			<td>PCR tube</td>
			<td>NIPPON Genetics</td>
			<td>FG-021D/SP</td>
			<td></td>
		</tr>
		<tr>
			<td>Petri dish</td>
			<td>AS ONE</td>
			<td>GD90-15</td>
			<td>Diameter 90 mm, height 15 mm.</td>
		</tr>
		<tr>
			<td>Photoresist</td>
			<td>AZ Electronic Materials</td>
			<td>AZ P4903</td>
			<td>AZ Electronic Materials was now acquired by Merck. AZ P4620 is an alternative.</td>
		</tr>
		<tr>
			<td>Plate reader</td>
			<td>BioTek</td>
			<td>POWERSCAN HT</td>
			<td></td>
		</tr>
		<tr>
			<td>Polyethelene gloves</td>
			<td>AS ONE</td>
			<td>6-896-02</td>
			<td>Trade name: Saniment.</td>
		</tr>
		<tr>
			<td>PURExpress in vitro protein synthesis kit</td>
			<td>New England Biolabs</td>
			<td>E6800S or E6800L</td>
			<td>For cell-free protein synthesis reaction.</td>
		</tr>
		<tr>
			<td>Reactive-ion etching system</td>
			<td>Samco</td>
			<td>RIE-10NR</td>
			<td>Other RIE systems are also applicable but should require optimization of RIE conditions (gas flow rate, chamber pressure, RF power, etching time, etc.)</td>
		</tr>
		<tr>
			<td>RNase inhibitor</td>
			<td>New England Biolabs</td>
			<td>M0314S</td>
			<td></td>
		</tr>
		<tr>
			<td>Scotch tape</td>
			<td>3M</td>
			<td>810-1-18D</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium hydroxide solution</td>
			<td>FUJIFILM Wako Pure Chemical</td>
			<td>194-09575</td>
			<td>8 M concentration; danger.</td>
		</tr>
		<tr>
			<td>Spin coater</td>
			<td>Oshigane</td>
			<td>SC-308</td>
			<td></td>
		</tr>
		<tr>
			<td>SURFLON S-386 surfactant</td>
			<td>AGC</td>
			<td>(Test sample)</td>
			<td>Free test sample may be available upon inquiry to AGC.</td>
		</tr>
		<tr>
			<td>SYLGARD 184 silicone elastomer</td>
			<td>Dow</td>
			<td>Sylgard184</td>
			<td>Chemical composition: polydimethylsiloxane. The default mixing ratio is base : curing agent = 10 : 1 (m/m).</td>
		</tr>
		<tr>
			<td>Tweezers</td>
			<td>Ideal-tek</td>
			<td>2WF.SA.1 
			2A</td>
			<td></td>
		</tr>
		<tr>
			<td>Ultrasonic cleaner</td>
			<td>AS ONE</td>
			<td>ASU-2M</td>
			<td></td>
		</tr>
		<tr>
			<td>Vacuum chuck</td>
			<td>Oshigane</td>
			<td>(Customized)</td>
			<td>Material: delrin; rectangular sample stage with multiple holes (48 holes, each with 1 mm diameter); the size is customzied to fit the size of the cover glass (24 mm &#215; 32 mm).</td>
		</tr>
	</tbody>
</table>

a femtoliter droplet array for massively parallel protein synthesis from single dna molecules

Advances in spatial resolution and detection sensitivity of scientific instrumentation make it possible to apply small reactors for biological and chemical research. To meet the demand for high-performance microreactors, we developed a femtoliter droplet array (FemDA) device and exemplified its application in massively parallel cell-free protein synthesis (CFPS) reactions. Over one million uniform droplets were readily generated within a finger-sized area using a two-step oil-sealing protocol. Every droplet was anchored in a femtoliter microchamber composed of a hydrophilic bottom and a hydrophobic sidewall. The hybrid hydrophilic-in-hydrophobic structure and the dedicated sealing oils and surfactants are crucial for stably retaining the femtoliter aqueous solution in the femtoliter space without evaporation loss. The femtoliter configuration and the simple structure of the FemDA device allowed minimal reagent consumption. The uniform dimension of the droplet reactors made large-scale quantitative and time-course measurements convincing and reliable. The FemDA technology correlated the protein yield of the CFPS reaction with the number of DNA molecules in each droplet. We streamlined the procedures about the microfabrication of the device, the formation of the femtoliter droplets, and the acquisition and analysis of the microscopic image data. The detailed protocol with the optimized low running cost makes the FemDA technology accessible to everyone who has standard cleanroom facilities and a conventional fluorescence microscope in their own place.

The microfabrication process consists of substrate cleaning, surface functionalization, CYTOP coating, photolithography, dry etching, photoresist stripping, and final cleaning. Importantly, the presented protocol allowed complete removal of the hydrophobic CYTOP polymer inside the microchambers Figure 3A), producing a highly parallel hydrophilic-in-hydrophobic structure on a standard cover glass substrate. With the aid of the oil sealing protocol, the uniform dimension of the resulting dropl...

Watch this Scientific Journal Video about A Femtoliter Droplet Array for Massively Parallel Protein Synthesis from Single DNA Molecules at JoVE.com

A Femtoliter Droplet Array for Massively Parallel Protein Synthesis from Single DNA Molecules

The overall goal of the protocol is to prepare over one million ordered, uniform, stable, and biocompatible femtoliter droplets on a 1 cm2 planar substrate that can be used for cell-free protein synthesis.

Advances in spatial resolution and detection sensitivity of scientific instrumentation make it possible to apply small reactors for biological and ...

More than one million uniform from the droplets are produced on the finger-sized substrate. And single DNA molecules are randomly distributed into each droplet. The protein yield is proportional to the number of the molecules in a droplet.Our technique can be used for a rapid and quantitative measurement of enzyme activity without complicated protein expression and purification. To begin, set a cover glass on a staining rack and place the rack in eight molar sodium hydroxide. Sonicate the cover glass and staining rack for 15 minutes at room temperature.Remove the staining rack from sodium hydroxide and rinse the cover glass with water 10 times. Dry the cover glass with an air gun. Then bake and dry the cover glass on a hot plate at 200 degree Celsius for five minutes.Prepare 0.05%aminosilane solution. Immerse the cover glass in this solution and incubate it for one hour at room temperature. Rinse the cover glass five times in pure water.Then dry the cover glass using an air gun. Bake it on the hot plate at 80 degree Celsius for five minutes. Place the cover glass substrate on a customized vacuum chuck for the spin coater.Dispense 70 to 90 microliters of type-A CYTOP polymer at the center of the glass substrate. Then immediately spin-coat the polymer. The initial polymer coating damage the quality of the final microchamber array.Dispense the polymer onto the center of the cover glass without introducing air bubbles. Pick up the coated glass by holding it at the corners and place it on an aluminum foil. Bake it for 30 minutes at 80 degree Celsius and then for another hour at 200 degree Celsius.Dispense 0.2 to 0.3 milliliters of photoresist at the center of the substrate. Immediately spin-coat the photoresist at 6, 000 rpm for 60 seconds. Use an ethanol-soaked wipe to remove the excess photoresist from the edges of the substrate.Bake the substrate at 110 degree Celsius for five minutes. To rehydrate the photoresist, let the substrate stand for 30 minutes at a relative humidity of 42 to 60%Load the substrate into the mask aligner and expose it for 25 seconds in a vacuum-contact mode. Then immerse the substrate in developer for five minutes to dissolve the exposed photoresist.Rinse the substrate 10 times using pure water. Then dry the substrate thoroughly using the air gun. Place the substrate in the reaction chamber of the reactive-ion etching machine and etch the photoresist covered CYTOP with the oxygen plasma.After etching, remove the remaining photoresist by sonicating the substrate in acetone for five minutes at room temperature. Then sonicate the substrate into propanol for five minutes. Rinse, sonicate, and rinse the substrate again using pure water as described in manuscript.Then dry the substrate with an air gun. Using a desktop cutter, cut double-coated adhesive Kapton film tape into the defined microchannel shapes. Stick the cut pieces of tape in the bottom of a flat Petri dish to serve as a master for the molding of the PDMS.Pour the PDMS mixture into the tape-patterned Petri dish. Then place the Petri dish into a mini vacuum chamber and deaerate the PDMS mixture for one to three hours. Then place the Petri dish in an oven at 60 degree Celsius and leave it overnight to cure the PDMS.After the PDMS has cured, peel the cured elastomer from the Petri dish and use a flat-cable cutter to cut out the PDMS microchannel blocks. Then punch a hole at each end of each microchannel. The previously prepared substrate will have an area for the microchamber array.Position the PDMS microchannel on this part of the substrate. Then insert a 200 microliter pipet tip into one of the holes in the PDMS microchannel. First, prepare the CFPS reaction solution in a PCR tube.Then, using a 200 microliter non-filter pipet tip, draw up 10 microliters of the solution. Insert the pipet tip into the inlet hole of the PDMS microchannel and push down on the pipet plunger until the solution overflows from the microchannel outlet. Transfer the FemDA device to a pre-chilled aluminum block.Confirm that the microchamber array area quickly turns from translucent to transparent. Draw 300 microliters of pre-chilled flush oil and immediately transfer the oil into the pipet tip of the microchannel inlet hole. The flush oil moves into the microchannel and extrudes the excess reaction solution located outside the microchambers.Simultaneously remove the two inserted pipet tips from the device. Immediately move the device from the aluminum block to paraffin film. Insert the prepared pipet tip containing the sealing oil into the inlet of the PDMS microchannel and inject the oil until it overflows from the outlet.The femtoliter droplets are sealed in individual microchambers by the oil. Open the defocused BF image. To remove smooth continuous backgrounds from every frame, select Subtract Background from the Process menu.Enter 20 for the rolling ball radius. Check the Preview box and select Okay. Select Yes when asked whether to process all images.Next, to reduce the noise, select Process, Filters, Median. Enter 2.0 for the radius in pixels. Check the Preview box and select Okay.Select Yes when asked whether to process all images. Next, select Image, Adjust, Threshold to separate the images of the microchambers from the background of the image. From the Plugins menu, select FemDA, FemDA Analysis.Input the approximate minimum and maximum numbers of pixels of a single microchamber. The expected minimum and maximum circularity of the microchambers and the start and end frame numbers, then select Generate ROI to detect the microchambers. The successfully detected ROIs are shown in the popup menu ROITable.In the FemDA Analysis window, select Apply ROI mask. Examine the image to see whether the microchambers were properly detected. Open the fluorescence image and bring it to the front.Click Apply ROI mask again to add the ROIs to the fluorescence image. In the FemDA Analysis window, select One-Shot to analyze image end-point data. Enter N for the Number of top pixels to use the top-end pixels of each ROI to calculate the mean intensity of the corresponding droplet.Then click Measure intensity to calculate the mean intensities of all detected droplets. The ROITable is updated with the new data from the fluorescence image and the histogram is displayed in a new window. Export the data by clicking the button Save as Text.Fluorescent solution was encapsulated in FemDA microchambers and the fluorescence intensity, which is correlated with droplet size was measured using microscopy. The droplets were found to have a narrow size distribution. The reconstructed 3D image from the confocal microscopy also showed the consistent droplet size over time.The droplets were stable at room temperature without evaporation loss or cross-contamination among droplets for at least 24-hours. The fluorescent protein mNeonGreen was synthesized in FemDA. And the stack image data was analyzed with the aid of the concurrent defocused bright field image.Because the fluorescence intensity of each droplet is measured of its protein yield, the histogram strongly suggests unequal numbers of DNA molecules per droplet. The probability of droplets containing different numbers of DNA molecules was a perfect fit to a Poisson distribution. Synthesis of the enzyme alkaline phosphatase was also carried out in FemDA with images captured every five minutes.The reaction showed a similar discreet distribution of the fluorescence intensity of the droplets at an earlier time points and the histogram results verified that the unequal numbers of the DNA molecules in the droplets. Single DNA molecule encapsulated in individual droplets can be further recovered, amplified, and sequenced make it highest proteins screening possible. A droplet technique featuring either small volume and either high stability allows for rapid and precise molecular diagnosis of cancer diseases with specific biomarkers.

a-femtoliter-droplet-array-for-massively-parallel-protein-synthesis

Research

JoVE Journal

Chemistry

10.1K Görüntüleme.  Japan Agency for Marine-Earth Science and Technology (JAMSTEC). Damlacıklardan bir milyondan fazla üniforma parmak büyüklüğünde substrat üzerinde üretilmektedir. Ve tek DNA molekülleri her damlacık içine rastgele dağıtılır. Protein verimi bir damlacıktaki molekül sayısıile orantılıdır.Tekniğimiz karmaşık protein ekspresyonu ve saflaştırma olmadan enzim aktivitesinin hızlı ve nicel ölçümü için kullanılabilir. Başlamak için, bir boyama raf üzerinde bir kapak cam ayarlayın ve sekiz azı lı sodyum hidroksit raf ...